About

Biography

I am board-certified in pediatric endocrinology and have been on the faculty of Cincinnati Children’s Hospital Medical Center and the University of Cincinnati since 2008. I completed my training in the United Kingdom, New Zealand, and Cincinnati. I serve as the medical director of the Cincinnati Children’s Differences of Sex Development (DSD) Center and the assistant director of the pediatric endocrinology fellowship training program.

I care for children and adolescents with a wide spectrum of endocrine conditions, including growth, puberty, thyroid, and adrenal disorders. I collaborate with interdisciplinary specialists to deliver the endocrine aspects of comprehensive and integrated care for patients with complex conditions. I lead the Cincinnati Children’s DSD Center, which provides interdisciplinary care for people born with conditions affecting reproductive development. The DSD Center is a member of the DSD-Translational Research Network, a national network that strives to optimize and standardize clinical practices and advance scientific knowledge in this field. I also serve as the primary endocrine consultant for the Cincinnati Comprehensive Neuromuscular Center. In conjunction with the neuromuscular team, I have helped pioneer global awareness of the importance of endocrine issues in patients affected by Duchenne Muscular Dystrophy.

MB, BCh: University of Wales College of Medicine, Cardiff, United Kingdom

FRACP: Royal Australasian College of Physicians, New Zealand

Residency: University Hospital of Wales, Cardiff, United Kingdom

Residency: Auckland Children's Hospital and Dunedin Hospital, Auckland and Dunedin, New Zealand

Residency: Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Fellowship: Pediatric Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Certifications: American Subspecialty Board of Pediatric Endocrinology, 2003, recertified 2013; American Board of Pediatrics, 2002; Fellow of the Royal Australasian College of Physicians (Pediatrics), 1995

Interests

Pediatric endocrinology, including growth, puberty, thyroid and adrenal disorders; differences of sex development, or conditions affecting reproductive development; endocrine and bone health in neuromuscular conditions

Interests

Differences of sex development; endocrine issues and bone health associated with Duchenne muscular dystrophy

Research Areas

Additional Languages

French, Mandarin

Insurance Information

Cincinnati Children's strives to accept a wide variety of health plans. Please contact your health insurance carrier to verify coverage for your specific benefit plan.

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Publications

Optimizing Care for Growth and Puberty in Duchenne Muscular Dystrophy: A Survey of Clinical Practice in the OPTIMIZE DMD Consortium. Wood, CL; Babalola, F; Benjamin, RW; Lam, C; Mcadam, L; Nicolau, S; Sbrocchi, AM; Scavina, M; Sorbara, JC; Ahmet, A; Weber, DR; Wong, SCJ; Crane, JL; Rutter, MM. Muscle and Nerve. 2026; 74(2):433-439.

Navigating sexual health, fertility, and adult wellness in individuals with Duchenne muscular dystrophy: Current standards of care and future directions. Nasomyont, N; Appel, A; Apkon, S; Hoskin, J; Surampudi, PN; Truba, N; Vargas, G; Veerapandiyan, A; Wood, CL; Moeschen, P; Ward, LM; Weber, DR; Choong Wong, S; Renthal, NE. Journal of Neuromuscular Diseases. 2026; 22143602261454423.

From X to Y and everything in between: navigating care for patients with 45,X/46,XY mosaicism. Johnson, J; Roberge, S; Hagood, B; Strine, A; Gutmark-Little, I; Pennesi, C; Hopkin, R; Breech, L; Schafer-Kalkhoff, T; Antommaria,, A; Rutter, M. Endocrine Abstracts. 2026.

Caring for Gender Diverse Youth With Duchenne Muscular Dystrophy: A Multisite Case Series. Melendez Garcia, CE; Ahmed, UA; Pagan, A; Appel, A; Nasomyont, N; Fiscaletti, M; Weber, DR; Crane, J; Apkon, S; Rutter, M; Wood, C; Ward, L; Renthal, NE. Pediatric Neurology. 2026; 179:87-90.

From case to caution: hyponatremia in a patient with Duchenne muscular dystrophy on vamorolone and lessons for clinicians. Murphy, C; Nasomyont, N; Tian, C; Ryan, TD; Villa, C; Reebals, L; Zygmunt, A; Rutter, MM. Neuromuscular Disorders. 2026; 62:106411.

The burden of bone disease in Duchenne muscular dystrophy: age-specific prevalence of osteoporosis and low bone density. Nasomyont, N; Tian, C; Hornung, L; Khoury, J; Wong, BL; Rutter, MM. Osteoporosis International. 2026; 37(5):1319-1328.

Acute Adverse Events Following Intravenous Bisphosphonate Infusion Are Uncommon in Patients With Duchenne Muscular Dystrophy Previously Treated With Oral Bisphosphonates. Nasomyont, N; Vilaisaktipakorn, P; Wasserman, H; Tian, C; Rutter, MM. Muscle and Nerve. 2026; 73(3):445-451.

Adrenal Suppression in Duchenne Muscular Dystrophy: Management Strategies Incorporating Novel Steroid Vamorolone. Sbrocchi, AM; Kinnett, K; Lautatzis, M-E; Mcmillan, HJ; Selby, KA; Veerapandiyan, A; Weber, DR; Apkon, S; Bharucha-Goebel, DX; Bharill, S; Ward, LM; Wood, CL; Wong, SC; Ahmet, A. Journal of the Endocrine Society. 2026; 10(2):bvaf181.

Defining Success in the Delivery of Fertility-Related Care for Patients with Differences of Sex Development. Streich-Tilles, T; Morrison, A; Schafer-Kalkhoff, T; Gardner, M; Suorsa-Johnson, KI; Baskin, A; Weidler, EM; Van Leeuwen, K; Sandberg, DE; Rutter, MM. Hormone Research in Paediatrics. 2026; 99(1):81-90.

MON-474 Adrenal Control in Pediatric 11β-Hydroxylase Deficient CAH Patients Using Different Hydrocortisone Formulations: A Two-Patient Case Study. Seo, P; Rutter, MM; Yau, M. Journal of the Endocrine Society. 2025; 9(Supplement_1):bvaf149.1731.

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